Food recall: Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6
Class III FDA enforcement event 61842. Recall start date: . Status in the FDA record: Terminated. Termination date: .
Reason for recall, in the words of FDA
The products contain synthetic equivalents of spermine and/or spermidine, which are constituents or extracts of an herb or other botanical, and the that a synthetic copy of a constituent or extract of an herb or other botanical is not a dietary ingredient, and such ingredients must be approved for use in supplements. The use has not been approved.
Class III, in the words of FDA
a situation in which use of or exposure to a violative product is not likely to cause adverse health consequences
H & L Jerch Sales, Inc. started this food recall on 11 Jun 2012. The firm address in the FDA record is in South Haven, MI. FDA put the recall in Class III. FDA event 61842 has 4 product records. The first FDA enforcement report date is 18 Jul 2012. The record gives the status Terminated, with the termination date 12 Feb 2013.
It is important to note that most of the time recall classifications are determined after the recalling firm provides all of the information needed to determine the risk posed to public health. The classification and posting in the FDA Enforcement Report should not be seen as an expansion or change to a firm’s voluntary public warning.
FDA publishes these words. Source: FDA, Enforcement Reports, Important Note, read on . openFDA export of .
Distribution
In the words of FDA.
Nationwide
Recalling firm
H & L Jerch Sales, Inc., South Haven, MI.
Recalling firm: The firm that the FDA record names for a recall.
FDA records how the recall started: Voluntary: Firm initiated.
Products
4 product records in the event.
| Recall number | Product | Quantity | Class | Status | Report date |
|---|---|---|---|---|---|
| F-1729-2012 | Product Name: Eroxil bottles of 30 tablets taken orally Nokomis Research Inc #6 | 50,604 bottles | Class III | Terminated | 18 Jul 2012 |
| F-1730-2012 | Erosyn bottles of 30 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #7 | 8260 bottles | Class III | Terminated | 18 Jul 2012 |
| F-1731-2012 | Fertalin bottles of 90 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #8 | 688 bottles | Class III | Terminated | 18 Jul 2012 |
| F-1732-2012 | Middle-Age Energy Booster bottles of 60 tablets taken orally Nokomis Research Inc Bell Lifestyle Products #65 | 1981 bottles | Class III | Terminated | 18 Jul 2012 |
openFDA, about the status: FDA does not update the status of a recall after the recall has been classified according to its level of hazard. As such, the status of a recall (open, completed, or terminated) will remain unchanged after published in the Enforcement Reports.
Source: openFDA, Drug Recall Enforcement Reports, Disclaimer.
Enforcement report: The FDA publication that lists recalls. It has one record for each product of a recall.
Enforcement event: All the product records that have one FDA event number. This site shows one event on one page.
Class III: The lowest of the three FDA recall classes.
The event in context
- Food events that started in 2012
- 515
- Share of these events in Class III
- 9%
- Product records in this event
- 4
- Events of the firm on the register
- 1
Official channels
- FDA enforcement report F-1729-2012The FDA record of the first product of this event.
- FDA: recalls, market withdrawals and safety alertsThe recall notices on the FDA site.
- FDA: report a problemThe FDA page that shows where a report about a product goes.
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Cite this page
Recall Register. FDA enforcement event 61842. https://recallregister.com/fda/iii/61842/. Source: openFDA enforcement reports. Data through .
Sources
- Source
- openFDA food enforcement reports
- Licence
- CC0 1.0
- Export date
- 28 Sep 2026
- Newest FDA report date on the register
- 23 Sep 2026
FDA has one record for each product. This site puts the records with the same event number on one page. The class of the event is the highest class of its records. How the register is made. Report an error.
Questions
- Where was the product distributed?
- The FDA record gives this distribution:
Nationwide
- What quantity of product is in FDA event 61842?
- The event has 4 product records. The first record gives this quantity:
50,604 bottles
- How did the recall start?
- The FDA record says:
Voluntary: Firm initiated
- How many food recalls of 2012 have the same class?
- 9% of the 515 food events that started in 2012 are in Class III.